Canonical Allele Identifier: CA401621844
Gene: FN3K HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.80708501T>G (hg19) chr17:g.82750625T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.82750625T>G , CM000679.2:g.82750625T>G GRCh38
NC_000017.10:g.80708501T>G , CM000679.1:g.80708501T>G GRCh37
NC_000017.9:g.78301790T>G NCBI36
NG_011721.1:g.3562T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000300784.8:c.800T>G MANE Select ENSP00000300784.7:p.Ile267Ser
ENST00000300784.7:c.800T>G ENSP00000300784.7:p.Ile267Ser
NM_022158.3:c.800T>G NP_071441.1:p.Ile267Ser
XM_024450872.1:c.650T>G XP_024306640.1:p.Ile217Ser
NM_022158.4:c.800T>G MANE Select NP_071441.1:p.Ile267Ser
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Search 100 bp 3'